Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.81478703A= , CM000670.2:g.81478703A= | GRCh38 |
| NC_000008.10:g.82390938A= , CM000670.1:g.82390938A= | GRCh37 |
| NC_000008.9:g.82553493A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256104.5:c.*162T= MANE Select | ENSP00000256104.4:n.*162T= | |
| ENST00000256104.4:c.*162T= | ENSP00000256104.4:n.*162T= | |
| ENST00000518669.5:n.496T= | ||
| ENST00000522659.1:c.*437T= | ENSP00000428385.1:n.*437T= | |
| NM_001442.2:c.*162T= | NP_001433.1:n.*162T= | |
| XR_001745980.1:n.514+16729A= | ||
| NM_001442.3:c.*162T= MANE Select | NP_001433.1:n.*162T= |